A citation-based method for searching scientific literature

Alain Martelli, Marie Wattenhofer-Donzé, Stéphane Schmucker, Samuel Bouvet, Laurence Reutenauer, Hélène Puccio. Hum Mol Genet 2007
Times Cited: 98







List of co-cited articles
1262 articles co-cited >1



Times Cited
  Times     Co-cited
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Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion.
V Campuzano, L Montermini, M D Moltò, L Pianese, M Cossée, F Cavalcanti, E Monros, F Rodius, F Duclos, A Monticelli,[...]. Science 1996
55

Mouse models for Friedreich ataxia exhibit cardiomyopathy, sensory nerve defect and Fe-S enzyme deficiency followed by intramitochondrial iron deposits.
H Puccio, D Simon, M Cossée, P Criqui-Filipe, F Tiziano, J Melki, C Hindelang, R Matyas, P Rustin, M Koenig. Nat Genet 2001
536
48

Aconitase and mitochondrial iron-sulphur protein deficiency in Friedreich ataxia.
A Rötig, P de Lonlay, D Chretien, F Foury, M Koenig, D Sidi, A Munnich, P Rustin. Nat Genet 1997
774
46

Regulation of mitochondrial iron accumulation by Yfh1p, a putative homolog of frataxin.
M Babcock, D de Silva, R Oaks, S Davis-Kaplan, S Jiralerspong, L Montermini, M Pandolfo, J Kaplan. Science 1997
726
32

Inactivation of the Friedreich ataxia mouse gene leads to early embryonic lethality without iron accumulation.
M Cossée, H Puccio, A Gansmuller, H Koutnikova, A Dierich, M LeMeur, K Fischbeck, P Dollé, M Koenig. Hum Mol Genet 2000
265
30

Friedreich ataxia: the oxidative stress paradox.
Hervé Seznec, Delphine Simon, Cécile Bouton, Laurence Reutenauer, Ariane Hertzog, Pawel Golik, Vincent Procaccio, Manisha Patel, Jean-Claude Drapier, Michel Koenig,[...]. Hum Mol Genet 2005
169
29



Iron-sulfur protein maturation in human cells: evidence for a function of frataxin.
Oliver Stehling, Hans-Peter Elsässer, Bernd Brückel, Ulrich Mühlenhoff, Roland Lill. Hum Mol Genet 2004
146
27



Histone deacetylase inhibitors reverse gene silencing in Friedreich's ataxia.
David Herman, Kai Jenssen, Ryan Burnett, Elisabetta Soragni, Susan L Perlman, Joel M Gottesfeld. Nat Chem Biol 2006
316
25

Mammalian frataxin: an essential function for cellular viability through an interaction with a preformed ISCU/NFS1/ISD11 iron-sulfur assembly complex.
Stéphane Schmucker, Alain Martelli, Florent Colin, Adeline Page, Marie Wattenhofer-Donzé, Laurence Reutenauer, Hélène Puccio. PLoS One 2011
176
25


The mitochondrial ATP-binding cassette transporter Abcb7 is essential in mice and participates in cytosolic iron-sulfur cluster biogenesis.
Corinne Pondarré, Brendan B Antiochos, Dean R Campagna, Stephen L Clarke, Eric L Greer, Kathryn M Deck, Alice McDonald, An-Ping Han, Amy Medlock, Jeffery L Kutok,[...]. Hum Mol Genet 2006
152
24

Frataxin is reduced in Friedreich ataxia patients and is associated with mitochondrial membranes.
V Campuzano, L Montermini, Y Lutz, L Cova, C Hindelang, S Jiralerspong, Y Trottier, S J Kish, B Faucheux, P Trouillas,[...]. Hum Mol Genet 1997
559
24

Oxidative stress in patients with Friedreich ataxia.
J B Schulz, T Dehmer, L Schöls, H Mende, C Hardt, M Vorgerd, K Bürk, W Matson, J Dichgans, M F Beal,[...]. Neurology 2000
246
23


Frataxin acts as an iron chaperone protein to modulate mitochondrial aconitase activity.
Anne-Laure Bulteau, Heather A O'Neill, Mary Claire Kennedy, Masao Ikeda-Saito, Grazia Isaya, Luke I Szweda. Science 2004
292
22

Structure, function, and formation of biological iron-sulfur clusters.
Deborah C Johnson, Dennis R Dean, Archer D Smith, Michael K Johnson. Annu Rev Biochem 2005
911
22


Friedreich ataxia: the clinical picture.
Massimo Pandolfo. J Neurol 2009
262
21


Assembly and iron-binding properties of human frataxin, the protein deficient in Friedreich ataxia.
Patrizia Cavadini, Heather A O'Neill, Oldrich Benada, Grazia Isaya. Hum Mol Genet 2002
163
20

Disabled early recruitment of antioxidant defenses in Friedreich's ataxia.
K Chantrel-Groussard, V Geromel, H Puccio, M Koenig, A Munnich, A Rötig, P Rustin. Hum Mol Genet 2001
157
19

Monomeric yeast frataxin is an iron-binding protein.
Jeremy D Cook, Krisztina Z Bencze, Ana D Jankovic, Anna K Crater, Courtney N Busch, Patrick B Bradley, Ann J Stemmler, Mark R Spaller, Timothy L Stemmler. Biochemistry 2006
101
19

Bacterial frataxin CyaY is the gatekeeper of iron-sulfur cluster formation catalyzed by IscS.
Salvatore Adinolfi, Clara Iannuzzi, Filippo Prischi, Chiara Pastore, Stefania Iametti, Stephen R Martin, Franco Bonomi, Annalisa Pastore. Nat Struct Mol Biol 2009
189
19

Mitochondrial iron detoxification is a primary function of frataxin that limits oxidative damage and preserves cell longevity.
Oleksandr Gakh, Sungjo Park, Gang Liu, Lee Macomber, James A Imlay, Gloria C Ferreira, Grazia Isaya. Hum Mol Genet 2006
161
18

Role of human mitochondrial Nfs1 in cytosolic iron-sulfur protein biogenesis and iron regulation.
Annette Biederbick, Oliver Stehling, Ralf Rösser, Brigitte Niggemeyer, Yumi Nakai, Hans-Peter Elsässer, Roland Lill. Mol Cell Biol 2006
130
18




In vivo maturation of human frataxin.
Ivano Condò, Natascia Ventura, Florence Malisan, Alessandra Rufini, Barbara Tomassini, Roberto Testi. Hum Mol Genet 2007
90
20

Mammalian frataxin controls sulfur production and iron entry during de novo Fe4S4 cluster assembly.
Florent Colin, Alain Martelli, Martin Clémancey, Jean-Marc Latour, Serge Gambarelli, Laura Zeppieri, Catherine Birck, Adeline Page, Hélène Puccio, Sandrine Ollagnier de Choudens. J Am Chem Soc 2013
110
18

The yeast frataxin homolog Yfh1p plays a specific role in the maturation of cellular Fe/S proteins.
Ulrich Mühlenhoff, Nadine Richhardt, Michael Ristow, Gyula Kispal, Roland Lill. Hum Mol Genet 2002
265
17

Increased levels of plasma malondialdehyde in Friedreich ataxia.
M Emond, G Lepage, M Vanasse, M Pandolfo. Neurology 2000
132
17

The human counterpart of zebrafish shiraz shows sideroblastic-like microcytic anemia and iron overload.
Clara Camaschella, Alessandro Campanella, Luigia De Falco, Loredana Boschetto, Roberta Merlini, Laura Silvestri, Sonia Levi, Achille Iolascon. Blood 2007
233
17

The Cfd1-Nbp35 complex acts as a scaffold for iron-sulfur protein assembly in the yeast cytosol.
Daili J A Netz, Antonio J Pierik, Martin Stümpfig, Ulrich Mühlenhoff, Roland Lill. Nat Chem Biol 2007
133
17

Elucidation of the mechanism of mitochondrial iron loading in Friedreich's ataxia by analysis of a mouse mutant.
Michael Li-Hsuan Huang, Erika M Becker, Megan Whitnall, Yohan Suryo Rahmanto, Prem Ponka, Des R Richardson. Proc Natl Acad Sci U S A 2009
161
17

Selective iron chelation in Friedreich ataxia: biologic and clinical implications.
Nathalie Boddaert, Kim Hanh Le Quan Sang, Agnès Rötig, Anne Leroy-Willig, Serge Gallet, Francis Brunelle, Daniel Sidi, Jean-Christophe Thalabard, Arnold Munnich, Z Ioav Cabantchik. Blood 2007
300
16

The hydrogenase-like Nar1p is essential for maturation of cytosolic and nuclear iron-sulphur proteins.
Janneke Balk, Antonio J Pierik, Daili J Aguilar Netz, Ulrich Mühlenhoff, Roland Lill. EMBO J 2004
155
16

Mitoferrin is essential for erythroid iron assimilation.
George C Shaw, John J Cope, Liangtao Li, Kenneth Corson, Candace Hersey, Gabriele E Ackermann, Babette Gwynn, Amy J Lambert, Rebecca A Wingert, David Traver,[...]. Nature 2006
397
16


GAA repeat expansion mutation mouse models of Friedreich ataxia exhibit oxidative stress leading to progressive neuronal and cardiac pathology.
Sahar Al-Mahdawi, Ricardo Mouro Pinto, Dhaval Varshney, Lorraine Lawrence, Margaret B Lowrie, Sian Hughes, Zoe Webster, Julian Blake, J Mark Cooper, Rosalind King,[...]. Genomics 2006
163
16

Friedreich's ataxia: point mutations and clinical presentation of compound heterozygotes.
M Cossée, A Dürr, M Schmitt, N Dahl, P Trouillas, P Allinson, M Kostrzewa, A Nivelon-Chevallier, K H Gustavson, A Kohlschütter,[...]. Ann Neurol 1999
262
16

Frataxin knockin mouse.
Carlos J Miranda, Manuela M Santos, Keiichi Ohshima, Julie Smith, Liangtao Li, Michaeline Bunting, Mireille Cossée, Michael Koenig, Jorge Sequeiros, Jerry Kaplan,[...]. FEBS Lett 2002
117
16



Frataxin deficiency alters heme pathway transcripts and decreases mitochondrial heme metabolites in mammalian cells.
Robert A Schoenfeld, Eleonora Napoli, Alice Wong, Shan Zhan, Laurence Reutenauer, Dexter Morin, Alan R Buckpitt, Franco Taroni, Bo Lonnerdal, Michael Ristow,[...]. Hum Mol Genet 2005
90
16

RNA silencing of the mitochondrial ABCB7 transporter in HeLa cells causes an iron-deficient phenotype with mitochondrial iron overload.
Patrizia Cavadini, Giorgio Biasiotto, Maura Poli, Sonia Levi, Rosanna Verardi, Isabella Zanella, Manuela Derosas, Rosaria Ingrassia, Marcella Corrado, Paolo Arosio. Blood 2007
129
15


Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.